Literature DB >> 22104698

Resveratrol inhibited GH3 cell growth and decreased prolactin level via estrogen receptors.

Chao Wang1, Zhi-qiang Hu, Ming Chu, Zhi Wang, Wei-guang Zhang, Lai-zang Wang, Chen-guang Li, Jun-sheng Wang.   

Abstract

AIMS: Pituitary prolactinoma is one of the estrogen-related tumors, some anti-estrogen compounds have suppressive effects on prolactinoma. Previous studies have suggested that resveratrol, a phytoestrogen, displays anti-estrogen and anti-tumor characteristics. Therefore, We determined whether resveratrol could inhibit the cell proliferation and decrease prolactin level in prolactinoma cell line, and identify the signaling pathways that mediate the effects of resveratrol. MAIN
METHODS: Prolactinoma cell line, GH3 cells were treated with resveratrol. Changes in proliferation, cell cycle, and apoptosis were assessed. The level of prolactin was assayed by Western blot or EIA. Expression of total Rb (retinoblastoma protein), phosphorylated Rb (pRb) and cyclin D3 were measured by Western blot. The changes of estrogen receptors and their roles in the effects of resveratrol were also determined. KEY
FINDINGS: We report that resveratrol had a dose-dependent inhibitory effect on GH3 cell proliferation. Inhibitory effects of resveratrol persisted, even on removal of resveratrol. The growth-inhibitory effect of resveratrol was accompanied by decreased expression of cyclin D3 and pRb. In addition, resveratrol induced G0/G1 cell cycle block and apoptosis. Furthermore, resveratrol suppressed intracellular levels and release of prolactin. Finally, we show that two types of estrogen receptor were involved in the different effects of resveratrol. SIGNIFICANCE: Taken together, we demonstrate that resveratrol could inhibit prolactinoma cell proliferation, induce cell cycle block and apoptosis, and decrease prolactin production and release, and estrogen receptors mediate its antitumor effects. And thus, these results lead us to propose developing resveratrol as a novel therapeutic agent for treatment of prolactinoma. Copyright Â
© 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 22104698     DOI: 10.1016/j.clineuro.2011.10.035

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  6 in total

1.  Combined effects of resveratrol and radiation in GH3 and TtT/GF pituitary adenoma cells.

Authors:  B Voellger; N Waldt; Rosita Rupa; E Kirches; O Melhem; H-J Ochel; C Mawrin; R Firsching
Journal:  J Neurooncol       Date:  2018-06-05       Impact factor: 4.130

Review 2.  Unraveling the Anticancer Effect of Curcumin and Resveratrol.

Authors:  Aline Renata Pavan; Gabriel Dalio Bernardes da Silva; Daniela Hartmann Jornada; Diego Eidy Chiba; Guilherme Felipe Dos Santos Fernandes; Chung Man Chin; Jean Leandro Dos Santos
Journal:  Nutrients       Date:  2016-11-10       Impact factor: 5.717

3.  Regulating the CCNB1 gene can affect cell proliferation and apoptosis in pituitary adenomas and activate epithelial-to-mesenchymal transition.

Authors:  Bin Li; Hai-Bo Zhu; Gui-Dong Song; Jian-Hua Cheng; Chu-Zhong Li; Ya-Zhuo Zhang; Peng Zhao
Journal:  Oncol Lett       Date:  2019-09-10       Impact factor: 2.967

4.  Resveratrol decreases B-cell lymphoma-2 expression and viability in GH3 pituitary adenoma cells of the rat.

Authors:  Benjamin Voellger; Elmar Kirches; Annette Wilisch-Neumann; Andreas Weise; Jorge Humberto Tapia-Perez; Rosita Rupa; Christian Mawrin; Raimund Firsching
Journal:  Onco Targets Ther       Date:  2013-09-16       Impact factor: 4.147

5.  Effects of resveratrol on cell growth and prolactin synthesis in GH3 cells.

Authors:  Wang Chao; Zhang Xuexin; Su Jun; Chu Ming; Jin Hua; Guofu Li; Chunlei Tan; Wanhai Xu
Journal:  Exp Ther Med       Date:  2014-02-13       Impact factor: 2.447

6.  Selective estrogen receptor modulators decrease invasiveness in pituitary adenoma cell lines AtT-20 and TtT/GF by affecting expression of MMP-14 and ADAM12.

Authors:  Zhuo Zhang; Jörg W Bartsch; Julia Benzel; Ting Lei; Christopher Nimsky; Benjamin Voellger
Journal:  FEBS Open Bio       Date:  2020-10-26       Impact factor: 2.792

  6 in total

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